• The tail of the sperm is used to maneuver for final penetration
of the ovum. • To fertilize an ovum, a sperm must first pass through the corona radiata and zona pellucida surrounding it. • The sperm penetrates the corona radiata by means of membrane-bound enzymes in the surface membrane that surrounds the head • Sperm can penetrate the zona pellucida only aft er binding with specifi c ZP3 receptors on the surface of this layer. Only sperm of the same species can bind to these zona pellucida sites and pass through Binding of sperm triggers the acrosome reaction, in which the acrosomal membrane disrupts and the acrosomal enzymes are released. The acrosomal enzymes digest the zona pellucida, enabling the sperm, with its tail still beating, to tunnel a path through this protective barrier. The first sperm to reach the ovum itself fuses with the plasma membrane of the ovum (actually a secondary oocyte), and its head (bearing its DNA) enters the ovum’s cytoplasm. The sperm’s tail is frequently lost in this process, but the head carries the crucial genetic information. Sperm–egg fusion triggers the exocytosis of enzyme-filled cortical granules that are located in the outermost, or cortical, region of the egg into the space between the egg membrane and the zona pellucida These enzymes diffuse into the zona pellucida, where they inactivate the ZP3 receptors so that other sperm reaching the zona pellucida cannot bind with it. The zona pellucida and seal off tunnels in progress to keep other penetrating sperm from advancing. These chemical changes in the ovum’s surrounding membrane makes this outer layer impenetrable to the entry of any more sperm, a phenomenon is known as block to polyspermy (“many sperm”). Sperm entry also triggers the second meiotic division of the egg, which is now ready to unite with the sperm to complete the fertilization process. Within an hour, the sperm and egg nuclei fuse, thanks to a molecular complex provided by the sperm that forms microtubules to bring the male and female chromosome sets together for uniting. In addition to contributing its half of the chromosomes to the fertilized ovum, now called a zygote, the victorious sperm activates ovum enzymes essential for the early embryonic developmental program. IMPLANTATION
• Th e zygote rapidly undergoes a number of mitotic cell divisions to form a
solid ball of cells called the morula. • During the first 6 to 8 days, while the developing embryo is in transit in the oviduct and floating in the uterine lumen, the rising levels of progesterone from the newly developed corpus luteum that formed after ovulation stimulate release of glycogen from the endometrium into the reproductive tract lumen for use as energy by the early embryo. • Th e nutrients stored in the cytoplasm of the ovum can sustain the embryo for less than a day. After that, the embryo relies on this secreted glycogen until implantation takes place. Meanwhile, the uterine lining is simultaneously being prepared for implantation under the influence of luteal-phase progesterone. During this time, the uterus is in its secretory, orprogestational phase, storing up glycogen and becoming richly vascularized. Placentation
• A blastocyst is a single-layer hollow ball of about 50 cells encircling a
fluid-filled cavity, with a dense mass of cells grouped together at one side. This dense mass, known as the inner cell mass, becomes the embryo and then fetus. The rest of the blastocyst is never incorporated into the fetus, instead serving a supportive role during intrauterine life. • The thin outermost layer, the trophoblast, accomplishes implantation,after which it develops into the fetal portion of the placenta. When the blastocyst is ready to implant, its surface becomes sticky. By this time, the endometrium is ready to accept the early embryo and it too has become more adhesive through increased formation of cell adhesion molecules (CAMs) that help “Velcro” the blastocyst when it first contacts the uterine lining. The blastocyst adheres to the uterine lining on the side of its inner cell mass. • Implantation begins when, on contact with the endometrium, the trophoblastic cells overlying the inner cell mass release protein- digesting enzymes. • These enzymes digest pathways between the endometrial cells, permitting fingerlike cords of trophoblastic cells to penetrate into the depths of the endometrium, where they continue to digest uterine cells . • Through its cannibalistic actions, the trophoblast performs the dual functions of accomplishing implantation as it carves out a hole in the endometrium for the blastocyst and making metabolic fuel and raw materials available for the developing embryo as the advancing trophoblastic projections break down the nutrient-rich endometrial tissue. • The plasma membranes of the advancing trophoblastic cells degenerate, forming a multinucleated syncytium that will eventually become the fetal portion of the placenta ascularization and enhanced nutrient storage. • The endometrial tissue so modified at the implantation site is called the decidua. It is into this super-rich decidual tissue that the blastocyst becomes embedded. • After the blastocyst burrows into the decidua by means of trophoblastic activity, a layer of endometrial cells covers over the surface of the hole, completely burying the blastocyst within the uterine lining . The trophoblastic layer continues to digest the surrounding decidual cells, providing energy for the embryo until the placenta develops. Placenta is composed of chorionic villi which provide a large contact area between the maternal and fetal circulations. In the mature placenta maternal blood enters the intervillous space by endometrial arteries and circulates around the villi to allow the gas and nutrient exchange. Deoxygenated blood leaves the intervillous space through endometrial veins. • Deoxygenated fetal blood comes to the chorionic villus by umbilical artery. Blood is oxygenated in the chorionic villi which is in a capillary structure. The oxygen and nutrient diffusion occurs through the villous capillary endothelial cells and thinned-out syncytiotrophoblast and cytotrophoblast. Then blood flows back to the fetus by a single umbilical vein. Fetal circulation